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Process Development Associate Jobs in Oxnard, CA

Process Development Sr Scientist

Thousand Oaks, CA · On-site

$96K - $131K/yr

Process Development Sr Scientist What you will do Let's do this. Let's change the world. In this ... OR Associate's degree and 8 years of directly related life science experience OR High school ...

Process Development Senior Scientist

Thousand Oaks, CA · On-site

$96K - $131K/yr

Process Development Senior Scientist What you will do Let's do this. Let's change the world. In ... OR Associate's degree and 8 years of Scientific experience OR High school diploma / GED and 10 ...

Process Development Associate Scientist What you will do Let's do this. Let's change the world. In this vital role you will contribute to our diverse early-stage portfolio projects that support ...

Process Development Associate Scientist What you will do Let's do this. Let's change the world. In this vital role you will contribute to our diverse early-stage portfolio projects that support ...

Associate Scientist The Associate Scientist within the Attribute Sciences Process Development Group performs analytical testing of process-related impurities to support the development of large ...

We are seeking a full-time, highly motivated Research Associate to join our growing bioprocess R&D ... Characterize process and quality attributes of cells during process development, either ...

We are seeking a full-time, highly motivated Research Associate to join our growing bioprocess R&D ... Characterize process and quality attributes of cells during process development, either ...

We are seeking a full-time, highly motivated Research Associate to join our growing bioprocess R&D ... Characterize process and quality attributes of cells during process development, either ...

Showing results 21-40

Process Development Associate information

See Oxnard, CA salary details

$20

$35

$52

How much do process development associate jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for process development associate in Oxnard, CA is $35.67, according to ZipRecruiter salary data. Most workers in this role earn between $29.28 and $43.80 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a process development associate?

To thrive as a Process Development Associate, you need a strong background in biochemistry, chemical engineering, or a related field, often supported by a bachelor’s or master’s degree. Experience with laboratory instrumentation, process optimization tools, and familiarity with regulatory standards such as GMP are typically required. Attention to detail, problem-solving abilities, and effective teamwork are vital soft skills for excelling in this role. These competencies are crucial for ensuring efficient process design, regulatory compliance, and successful scale-up in manufacturing environments.

What are the primary challenges faced by a process development associate when scaling up laboratory processes to manufacturing scale?

A Process Development Associate often encounters challenges in translating small-scale laboratory protocols into large-scale manufacturing processes. Variations in equipment, raw material quality, and environmental conditions can impact reproducibility and efficiency. Addressing these issues requires strong troubleshooting skills, attention to detail, and close collaboration with cross-functional teams such as manufacturing, quality assurance, and engineering to ensure smooth technology transfer and consistent product quality.

What is the difference between Process Development Associate vs Process Engineer?

AspectProcess Development AssociateProcess Engineer
Required CredentialsBachelor's in Chemistry, Chemical Engineering, or related field; often some experience in process developmentBachelor's or Master's in Chemical Engineering or related; more emphasis on engineering principles
Work EnvironmentLaboratory and pilot plant settings, focused on process research and developmentManufacturing plants, production lines, and process optimization environments
Employer & Industry UsagePharmaceutical, biotech, and chemical industries; entry to mid-level rolesChemical, manufacturing, and process industries; more senior roles in process optimization

The Process Development Associate primarily focuses on developing and optimizing new processes in lab and pilot settings, often working closely with R&D teams. In contrast, the Process Engineer applies engineering principles to scale up processes, improve manufacturing efficiency, and troubleshoot production issues. While both roles require a background in chemical or process engineering, the Process Development Associate is more research-oriented, whereas the Process Engineer emphasizes process implementation and optimization in production environments.

What is a process development associate job description?

A process development associate is responsible for designing, testing, and optimizing manufacturing or operational processes to improve efficiency, quality, and safety. They often work with cross-functional teams, utilize data analysis tools, and follow regulatory standards to develop scalable processes. Strong problem-solving skills and knowledge of industry-specific regulations are essential for this role.

What is a process development associate?

A process development associate is a professional responsible for designing, testing, and optimizing manufacturing or operational processes to improve efficiency, quality, and cost-effectiveness. They often work with cross-functional teams, utilize data analysis tools, and may require knowledge of regulatory standards and process validation techniques.

What job categories do people searching Process Development Associate jobs in Oxnard, CA look for?

The top searched job categories for Process Development Associate jobs in Oxnard, CA are:

What cities near Oxnard, CA are hiring for Process Development Associate jobs?

Cities near Oxnard, CA with the most Process Development Associate job openings:

Infographic showing various Process Development Associate job openings in Oxnard, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $74,193 per year, or $35.7 per hour.

Process Development Associate Scientist - Pre-Pivotal Drug Product Technologies

Thousand Oaks, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 2 days ago


Job description

Career Category
Operations
Job Description
Join Amgen's Mission of Serving Patients
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Process Development Associate Scientist
What you will do
Let's do this. Let's change the world. In this vital role you will join Pre-Pivotal Drug Product Technologies group, responsible for early-stage drug product development across diverse modalities, with a strong emphasis on monoclonal antibodies, multispecifics and other biologic modalities. The role involves designing and developing liquid and lyophilized formulations; evaluating critical quality attributes (CQAs); establishing robust, scalable fill/finish processes for complex biologic drug products; and authoring and supporting high quality regulatory submissions.
  • Plan and execute formulation, stability, end-use compatibility, and fill/finish process studies for early-stage programs.
  • Develop and characterize liquid and lyophilized formulations for biologics, with particular emphasis on biologics drug product formulation, handling, and lab-scale sterile filling.
  • Investigate biologics-relevant CQAs (e.g., aggregation, fragmentation, charge/size variants, subvisible particles, surface interactions) to inform formulation and process design decisions.
  • Design, develop, and execute automated high-throughput formulation screening workflows to accelerate excipient selection, formulation optimization, and processability assessments.
  • Develop and implement laboratory automation solutions, including robotic liquid handling systems and automated sample preparation workflows, to improve experimental throughput, reproducibility, and data quality.
  • Utilize design of experiments (DoE), high-throughput experimentation, and automated data analysis pipelines to efficiently explore formulation design space and support data-driven decision making.
  • Identify and address technology gaps impacting biologics stability, protein-excipient interactions, and process-related stress responses.
  • Apply machine learning, AI, laboratory automation, and data science to predictive modeling, workflow acceleration, and decision-making.
  • Author/review guideline documents, technical protocols, technical transfer documentation, reports, product impact assessments, and regulatory sections in support of IND submissions
  • Meticulous data collection, documentation using electronic data capture systems
  • Ability to work in a matrixed team and present data cross functionally

What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.
Basic Qualifications:
Master's degree
OR
Bachelor's degree and 2 years of Scientific experience
OR
Associate's degree and 4 years of Scientific experience
OR
High school diploma / GED and 6 years of Scientific experience
Preferred Qualifications:
  • Master's degree in Pharmaceutics, Biotechnology, Biochemistry, Physical Biochemistry, Biophysics, Chemical Engineering, or related field with a minimum of 3+ years of industrial experience in pharmaceutical/biotechnology or related field
  • Understanding of physical/chemical stability of proteins and how process related stress impacts product quality.
  • Preferred experience in biophysical analysis (Light scattering, DSF, AUC, FFF) and mass spectrometry (peptide mapping).
  • Ability to learn and act on dynamic information at a rapid pace, hard-working and collaborative attitude
  • Excellent oral and written communication skills for timely documentation, presentation, and discussion of scientific results for a fast pace and cross functional environment.
  • Proven experience in formulation development and fill/finish operations for biologics; direct biologics drug product formulation experience is strongly preferred.
  • Hands-on experience with high-throughput formulation development, automated liquid handling systems (e.g., Hamilton, Tecan, Beckman Coulter, Opentrons, or equivalent), and robotic laboratory workflows.
  • Experience implementing laboratory automation, workflow digitization, and electronic data capture to improve R&D productivity.
  • Familiarity with DoE, high-throughput experimentation, laboratory robotics, and workflow orchestration for formulation and process development.
  • Strong foundation in analytical techniques relevant to biologics and biologics (e.g., UPLC/HPLC, SEC, IEX, RP-HPLC, HIC, CE-SDS, subvisible particle analysis, etc.).

What you can expect from us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Salary Range
90,442.55USD -122,363.45 USD